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Motoshi Kikuchi

Researcher at Jichi Medical University

Publications -  73
Citations -  1920

Motoshi Kikuchi is an academic researcher from Jichi Medical University. The author has contributed to research in topics: Anterior pituitary & Pituitary gland. The author has an hindex of 20, co-authored 71 publications receiving 1754 citations. Previous affiliations of Motoshi Kikuchi include Waseda University.

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A novel avian hypothalamic peptide inhibiting gonadotropin release.

TL;DR: It is shown, in a bird, that the hypothalamus also contains a novel peptide which inhibits gonadotropin release, the first hypothalamic peptide inhibiting gonadotropic hormone reported in a vertebrate.
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The adrenocortical response of tufted puffin chicks to nutritional deficits.

TL;DR: The hypothesis that puffin chicks suppress HPA-axis activity in response to short- and long-term nutritional deficits may allow a chick to extend its development in the nest, while eluding detrimental effects of chronic cort elevation.
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Reproductive development according to elevation in a seasonally breeding male songbird.

TL;DR: In this article, the authors demonstrate variation in reproductive timing across small geographic distances by examining the vernal testicular recrudescence of adult song sparrows (Melospiza melodia morphna) breeding in coastal and montane habitats.
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Living-cell imaging of transgenic rat anterior pituitary cells in primary culture reveals novel characteristics of folliculo-stellate cells

TL;DR: The novel characteristics of FS cells observed in the present study suggest that in the anterior pituitary gland, FS cells play important roles in determining and/or maintaining local cellular arrangement in the presence of ECM components.
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Expression of Chemokine CXCL12 and Its Receptor CXCR4 in Folliculostellate (FS) Cells of the Rat Anterior Pituitary Gland: The CXCL12/CXCR4 Axis Induces Interconnection of FS Cells

TL;DR: This study attempted to discover the factor that induces interconnection of FS cells and succeeded in identifying chemokine (CXC)-L12 and its receptor CXCR4 as potential candidate molecules.